CCND1, cyclin D1, 595

N. diseases: 859; N. variants: 12
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C0730303
Disease: Capillary hemangioma of retina
Capillary hemangioma of retina
disease Neoplasms; Cardiovascular Diseases Neoplastic Process 15 1 0.100 None 0
CUI: C0746674
Disease: Generalized muscle weakness
Generalized muscle weakness
phenotype Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases Sign or Symptom 126 4 0.100 None 0
CUI: C4048270
Disease: Decreased antibody level in blood
Decreased antibody level in blood
phenotype Finding 75 5 0.100 None 0
CUI: C1963077
Disease: Bone Pain, CTCAE 3.0
Bone Pain, CTCAE 3.0
phenotype Finding 67 0.100 None 0
CUI: C0030554
Disease: Paresthesia
Paresthesia
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 121 8 0.100 None 0
CUI: C0544886
Disease: Somatic mutation
Somatic mutation
phenotype Cell or Molecular Dysfunction 151 0.100 None 0
Abnormality of blood and blood-forming tissues
disease Finding 23 1 0.100 None 0
CUI: C0032227
Disease: Pleural effusion disorder
Pleural effusion disorder
group Respiratory Tract Diseases Disease or Syndrome 227 14 0.100 None 0
CUI: C0032461
Disease: Polycythemia
Polycythemia
disease Hemic and Lymphatic Diseases Disease or Syndrome 82 22 0.100 None 0
CUI: C2609414
Disease: Acute kidney injury
Acute kidney injury
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Injury or Poisoning 185 3 0.100 None 0
CUI: C0020437
Disease: Hypercalcemia
Hypercalcemia
disease Nutritional and Metabolic Diseases Disease or Syndrome 157 9 0.100 None 0
CUI: C0016663
Disease: Pathological fracture
Pathological fracture
phenotype Wounds and Injuries Pathologic Function 35 2 0.100 None 0
COLORECTAL CANCER, SUSCEPTIBILITY TO
phenotype Finding 3 8 0.100 None 0 1
CUI: C0700225
Disease: Serum creatinine raised
Serum creatinine raised
phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Finding 27 2 0.100 None 0
CUI: C4021780
Disease: Abnormality of the liver
Abnormality of the liver
phenotype Finding 75 8 0.100 None 0
CUI: C0029453
Disease: Osteopenia
Osteopenia
disease Nutritional and Metabolic Diseases; Musculoskeletal Diseases Disease or Syndrome 845 61 0.100 None 0
Functional abnormality of the gastrointestinal tract
phenotype Pathologic Function 7 0.100 None 0
Abnormality of the gastrointestinal tract
phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Anatomical Abnormality 14 1 0.100 None 0
Papillary cystadenoma of the epididymis
disease Neoplastic Process 6 0.100 None 0
CUI: C4024223
Disease: Spinal hemangioblastoma
Spinal hemangioblastoma
disease Neoplasms; Nervous System Diseases Neoplastic Process 2 1 0.100 None 0
CUI: C0030283
Disease: Pancreatic Cyst
Pancreatic Cyst
disease Digestive System Diseases; Neoplasms Disease or Syndrome 60 4 0.100 None 0
Abnormality of bone marrow cell morphology
disease Anatomical Abnormality 15 0.100 None 0
CUI: C0030489
Disease: Paraproteinemias
Paraproteinemias
disease Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 14 9 0.100 None 0
MULTIPLE MYELOMA, t(11;14) TYPE, SUSCEPTIBILITY TO
phenotype Finding 1 1 0.100 None 0 1
CUI: C1332900
Disease: Cerebellar hemangioblastoma
Cerebellar hemangioblastoma
disease Neoplasms; Nervous System Diseases Neoplastic Process 6 4 0.100 None 0